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An acute increase in Left Atrial volume and left ventricular filling pressure during Adenosine administered myocardial hyperaemia: CMR First-Pass Perfusion Study

OBJECTIVE: To investigate whether left atrial (LA) volume and left ventricular filling pressure (LVFP) assessed by cardiovascular magnetic resonance (CMR) change during adenosine delivered myocardial hyperaemia as part of a first-pass stress perfusion study. METHODS AND RESULTS: We enrolled 33 patie...

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Autores principales: Garg, Pankaj, Javed, Wasim, Assadi, Hosamadin, Alabed, Samer, Grafton-Clarke, Ciaran, Swift, Andrew J, Williams, Gareth, Al-Mohammad, Abdallah, Sawh, Chris, Vassiliou, Vassilios S, Khanji, Mohammed Y, Ricci, Fabrizio, Greenwood, John P, Plein, Sven, Swoboda, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10176699/
https://www.ncbi.nlm.nih.gov/pubmed/37170253
http://dx.doi.org/10.1186/s12872-023-03230-x
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author Garg, Pankaj
Javed, Wasim
Assadi, Hosamadin
Alabed, Samer
Grafton-Clarke, Ciaran
Swift, Andrew J
Williams, Gareth
Al-Mohammad, Abdallah
Sawh, Chris
Vassiliou, Vassilios S
Khanji, Mohammed Y
Ricci, Fabrizio
Greenwood, John P
Plein, Sven
Swoboda, Peter
author_facet Garg, Pankaj
Javed, Wasim
Assadi, Hosamadin
Alabed, Samer
Grafton-Clarke, Ciaran
Swift, Andrew J
Williams, Gareth
Al-Mohammad, Abdallah
Sawh, Chris
Vassiliou, Vassilios S
Khanji, Mohammed Y
Ricci, Fabrizio
Greenwood, John P
Plein, Sven
Swoboda, Peter
author_sort Garg, Pankaj
collection PubMed
description OBJECTIVE: To investigate whether left atrial (LA) volume and left ventricular filling pressure (LVFP) assessed by cardiovascular magnetic resonance (CMR) change during adenosine delivered myocardial hyperaemia as part of a first-pass stress perfusion study. METHODS AND RESULTS: We enrolled 33 patients who had stress CMR. These patients had a baseline four-chamber cine and stress four-chamber cine, which was done at peak myocardial hyperaemic state after administering adenosine. The left and right atria were segmented in the end ventricular diastolic and systolic phases. Short-axis cine stack was segmented for ventricular functional assessment. At peak hyperaemic state, left atrial end ventricular systolic volume just before mitral valve opening increased significantly from baseline in all (91 ± 35ml vs. 81 ± 33ml, P = 0.0002), in males only (99 ± 35ml vs. 88 ± 33ml, P = 0.002) and females only (70 ± 26ml vs. 62 ± 22ml, P = 0.02). The right atrial end ventricular systolic volume increased less significantly from baseline (68 ± 21ml vs. 63 ± 20ml, P = 0.0448). CMR-derived LVFP (equivalent to pulmonary capillary wedge pressure) increased significantly at the peak hyperaemic state in all (15.1 ± 2.9mmHg vs. 14.4 ± 2.8mmHg, P = 0.0002), females only (12.9 ± 2.1mmHg vs. 12.3 ± 1.9mmHg, P = 0.029) and males only (15.9 ± 2.8mmHg vs. 15.2 ± 2.7mmHg, P = 0.002) cohorts. CONCLUSION: Left atrial volume assessment by CMR can measure acute and dynamic changes in preloading conditions on the left ventricle. During adenosine administered first-pass perfusion CMR, left atrial volume and LVFP rise significantly.
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spelling pubmed-101766992023-05-13 An acute increase in Left Atrial volume and left ventricular filling pressure during Adenosine administered myocardial hyperaemia: CMR First-Pass Perfusion Study Garg, Pankaj Javed, Wasim Assadi, Hosamadin Alabed, Samer Grafton-Clarke, Ciaran Swift, Andrew J Williams, Gareth Al-Mohammad, Abdallah Sawh, Chris Vassiliou, Vassilios S Khanji, Mohammed Y Ricci, Fabrizio Greenwood, John P Plein, Sven Swoboda, Peter BMC Cardiovasc Disord Research OBJECTIVE: To investigate whether left atrial (LA) volume and left ventricular filling pressure (LVFP) assessed by cardiovascular magnetic resonance (CMR) change during adenosine delivered myocardial hyperaemia as part of a first-pass stress perfusion study. METHODS AND RESULTS: We enrolled 33 patients who had stress CMR. These patients had a baseline four-chamber cine and stress four-chamber cine, which was done at peak myocardial hyperaemic state after administering adenosine. The left and right atria were segmented in the end ventricular diastolic and systolic phases. Short-axis cine stack was segmented for ventricular functional assessment. At peak hyperaemic state, left atrial end ventricular systolic volume just before mitral valve opening increased significantly from baseline in all (91 ± 35ml vs. 81 ± 33ml, P = 0.0002), in males only (99 ± 35ml vs. 88 ± 33ml, P = 0.002) and females only (70 ± 26ml vs. 62 ± 22ml, P = 0.02). The right atrial end ventricular systolic volume increased less significantly from baseline (68 ± 21ml vs. 63 ± 20ml, P = 0.0448). CMR-derived LVFP (equivalent to pulmonary capillary wedge pressure) increased significantly at the peak hyperaemic state in all (15.1 ± 2.9mmHg vs. 14.4 ± 2.8mmHg, P = 0.0002), females only (12.9 ± 2.1mmHg vs. 12.3 ± 1.9mmHg, P = 0.029) and males only (15.9 ± 2.8mmHg vs. 15.2 ± 2.7mmHg, P = 0.002) cohorts. CONCLUSION: Left atrial volume assessment by CMR can measure acute and dynamic changes in preloading conditions on the left ventricle. During adenosine administered first-pass perfusion CMR, left atrial volume and LVFP rise significantly. BioMed Central 2023-05-11 /pmc/articles/PMC10176699/ /pubmed/37170253 http://dx.doi.org/10.1186/s12872-023-03230-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Garg, Pankaj
Javed, Wasim
Assadi, Hosamadin
Alabed, Samer
Grafton-Clarke, Ciaran
Swift, Andrew J
Williams, Gareth
Al-Mohammad, Abdallah
Sawh, Chris
Vassiliou, Vassilios S
Khanji, Mohammed Y
Ricci, Fabrizio
Greenwood, John P
Plein, Sven
Swoboda, Peter
An acute increase in Left Atrial volume and left ventricular filling pressure during Adenosine administered myocardial hyperaemia: CMR First-Pass Perfusion Study
title An acute increase in Left Atrial volume and left ventricular filling pressure during Adenosine administered myocardial hyperaemia: CMR First-Pass Perfusion Study
title_full An acute increase in Left Atrial volume and left ventricular filling pressure during Adenosine administered myocardial hyperaemia: CMR First-Pass Perfusion Study
title_fullStr An acute increase in Left Atrial volume and left ventricular filling pressure during Adenosine administered myocardial hyperaemia: CMR First-Pass Perfusion Study
title_full_unstemmed An acute increase in Left Atrial volume and left ventricular filling pressure during Adenosine administered myocardial hyperaemia: CMR First-Pass Perfusion Study
title_short An acute increase in Left Atrial volume and left ventricular filling pressure during Adenosine administered myocardial hyperaemia: CMR First-Pass Perfusion Study
title_sort acute increase in left atrial volume and left ventricular filling pressure during adenosine administered myocardial hyperaemia: cmr first-pass perfusion study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10176699/
https://www.ncbi.nlm.nih.gov/pubmed/37170253
http://dx.doi.org/10.1186/s12872-023-03230-x
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